A study of Italian pediatric celiac disease patients confirms that the primary HLA association is to the DQ(α1∗0501, β1∗0201) heterodimer
- 29 February 1992
- journal article
- Published by Elsevier in Human Immunology
- Vol. 33 (2) , 133-139
- https://doi.org/10.1016/0198-8859(92)90064-t
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A family study confirms that the HLA-DP associations with celiac disease are the result of an extended HLA-DR3 haplotypeHuman Immunology, 1991
- Reassessment of HLA association with celiac disease in special reference to the DP associationHuman Immunology, 1990
- A gene in the human major histocompatibility complex class II region controlling the class I antigen presentation pathwayNature, 1990
- Susceptibility to develop celiac disease is primarily associated with HLA-DQ allelesHuman Immunology, 1990
- Celiac disease is associated with an extended HLA-DR3 haplotype which includes HLA-DPw1Human Immunology, 1990
- Restriction fragment length polymorphism in HLA class II genes of Latin-American caucasian celiac disease patientsHuman Immunology, 1989
- An HLA-DQ alpha allele identified at DNA and protein level is strongly associated with celiac diseaseHuman Immunology, 1988
- A radioimmunoassay typing study of non-DQw2-associated celiac diseaseClinical Immunology and Immunopathology, 1986
- Evidence that celiac disease is primarily associated with a DC locus allelic specificityClinical Immunology and Immunopathology, 1983
- ON ESTIMATING THE RELATION BETWEEN BLOOD GROUP AND DISEASEAnnals of Human Genetics, 1955